Epidemiology Flashcards

(48 cards)

1
Q

what is prevalence

A

the number of existing cases in a population at a designated time

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2
Q

what is incidence

A

the number of new cases

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3
Q

relationship between prevalence and incidence

A

prevalence = incidence x average disease duration

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4
Q

name the three types of population pyramid

A

-spike - high birth rate, high death rate
-wedge - high birth rate, low death rate, high growth rate
-barrel - low birth rate, low death rate

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5
Q

what is infant mortality rate

A

no. of deaths of infants aged 0-1years/no. live births

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6
Q

what is a total period fertility rate (TPFR)

A

the average number of children that would be born to a woman over her lifetime

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7
Q

define life expectancy

A

the number of years a baby born today can be expected to live if it experienced the current age-specific mortality rates

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8
Q

what is healthy life expectancy

A

expected years of life in good or fairly good general health

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9
Q

what is the PYLL index

A

potential years of life lost
-a measure of the relative impact of various diseases and lethal forces on society
(the number of years of life lost when a person dies prematurely)

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10
Q

what is dependency ratio

A

a demographic measure of the ratio of the number of dependents to the total working age population in a country or region

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11
Q

how do you calculate dependency ratio

A

under 15 plus over 65 years/population ages 15-64 years

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12
Q

what’s a cross sectional study

A

estimate frequency or outcome at a particular point in time
-descriptive or analytical

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13
Q

why do a cross sectional study?

A

-health service planning - prevalence of specific outcome in a defined population at a point in time
-useful for assessing burden of disease and planning preventative and curative services
-not useful for rare diseases
-generate hypotheses about causes
(these studies prove association not causation)

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14
Q

survey sampling

A

-can make statements about the population by asking a (small) sample
-a well taken sample is (almost) as informative as a complete census
-sampling is a feature of all research designs

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15
Q

what is simple random sampling

A

-list the group
-generate random numbers
-contact selected individuals
-collect data

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16
Q

what bias in cross-sectional studies

A

-selection bias (characteristics of those taking part vs those not taking part)
-information bias (recall bias)

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17
Q

advantages of cross sectional

A

-easy and economical
-provides important information on the distribution and burden of exposures and outcomes - health service planning
-can be used as the first step in the study of a possible exposure-outcome relationship

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18
Q

weaknesses of cross sectional

A

-limited value for investigating aetiological relationships
-can be difficult to establish the time-sequence of events, the exposure may have occurred as a result of the outcome (reverse causality)
-not good for rare diseases
-selection bias (characteristics of those taking part/not taking part)
-recall bias
-could generate hypotheses about causes

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19
Q

what is an ecological study

A

observational study with populations or groups (instead of individuals) being unit of observation

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20
Q

what are the uses of an ecological study

A

-described association at group level
-quick and cheap - routine data
-generates hypotheses - first step
-some risk factors may not easily be measurable at an individual level

21
Q

what is ecological fallacy

A

-ecological studies enable us to make ecological inferences about effects at the group-level
-they do not enable us to make inferences about individual risks
-an attempt to infer from the ecological level to the individual level is often called an ecological fallacy

22
Q

purpose of randomised control trials

A

-minimise selection bias
-minimise confounding
-if participants are blind to treatment allocation then reporting bias is minimised
-if investigators are blind to allocation then observer bias is minimised
-provides powerful evidence of a causal relationship between the intervention and the outcome

23
Q

what is incidence risk

A

the number of new cases in interval/population initially at risk

24
Q

what is incidence rate

A

the number of new cases/total person-time at risk

25
what is incidence rate good for
dynamic populations
26
what is incidence risk good for
static populations
27
what is annual incidence
counts the deaths over a calendar year
28
what is cumulative incidence
frequency of new cases over a specified period
29
what to consider when deciding if risk factor and disease is causal (10 marks)
-consider relative risk, hazard ratio and odds ratio to determine strength of association -attributable risk -define causation and association -consider that aetiology of chronic disease is often difficult to determine -some exposures may cause more than one outcome -outcomes may be due to multiple exposures or continual exposure over time -causes may differ by individual -probabilistic causation is when causal factor increases the chance of disease -a sufficient cause is a complete causal mechanism that always produces disease
30
case control main features, advantages and disadvantages (10 marks)
-measure exposure in cases vs controls -select (diseased) cases and (undiseased) controls -use odds ratio to interpret results -selection bias can occur as people who participate are only those who are eligible -observer bias can occur if knowledge of case/control status -same with participant bias -there can be rare outcomes -time varying exposures -can assess multiple exposures -there wouldn't be any recall bias -can prove a good causal relationship between exposure and outcome
31
advantages of case-control studies
-no recall bias -can show rare outcomes (from rare diseases) -can look at multiple exposures/risk factors simultaneously -time varying exposures -quick, inexpensive and easy -useful initial studies to establish an association
32
ecological fallacy 6 marker
-can happen in ecological studies -define ecological studies -ecological fallacy occurs when a researcher attempts to infer from the ecological level to the individual level -ecological studies do not enable us to make inferences about individual risks -there are complex associations between disease and exposure -countries with high or low exposure differ systematically in many other ways
33
what does it mean if p<0.05
reject chance -conclude real effect
34
what does it mean if p>0.05
cannot exclude chance -cannot conclude there is real effect
35
advantages of randomised control trials
-minimises selection bias and confounding -if participant blind to allocation then minimises reporter bias -if observer blind to allocation then minimises observer bias -multiple outcomes can be examined -incidence rate of outcome can be measured
36
disadvantages of randomised control trials
-very time consuming - trials can take years -recruitment is difficult and time consuming -impossible to do interventional trials sometimes -expensive
37
advantages of cohort studies
-temporality - exposure status defined before outcome -can measure multiple outcomes from rare exposures -no recall bias -its possible to estimate all measures of incidence and effect
37
disadvantages of cohort studies
-huge investment of time, human resources and financial resources -reproducibility is hard -loss to follow up - bias can be introduced which is difficult to control -requires large sample size -uncontrolled confounding variables -inefficient for rare diseases
38
two types of information bias
reporter and observer
39
reporting bias
-when subjects give an answer they think will please the investigator -when subjects conceal potentially embarrassing info -when subject with a specific health outcome report previous exposure with a different degree of accuracy to other subjects -when subject who have experienced a specific exposure report subsequent health events to a different degree of accuracy to others
40
how can you avoid/minimise reporting bias
-use exposure data before outcome -objective data sources where possible -keep subjects unaware of association under study
41
what is observer bias
-when accuracy of exposure data recorded by investigator differs (case control and cross sectional) -when accuracy of outcome data differs (cohort and intervention studies) -interviewer bias
42
how do you avoid/minimise observer bias?
-the people who are responsible for classifying the outcome do not know the subjects' exposure category -blinding
43
intention to treat
-compares outcomes for all randomised individuals (even if they stop taking treatment or drop out of study) -assesses the overall effect of assigning a subject to receive a particular intervention -analysis is the most important analysis as intervention and control groups compared as originally randomised -more likely to underestimate treatment effect (in randomised control trials lecture)
44
short notes on incidence risk and rate (6 marks)
-incidence measures number of new cases in a group/population -incidence risk is number of new cases in an interval/population initially at risk -incidence risk is good for static populations -incidence rate is number of new cases /total person-time at risk -incidence rate measures the rate at which a new disease occured over a period of time -incidence rate is good for dynamic populations -annual incidence counts deaths over a calendar year -cumulative incidence is the frequency of new cases over a specified period
45
Cluster sampling | 6 mark short notes
-cluster sampling involves dividing a population into clusters and then randomly selecting a sample of these clusters -clusters are randomised -there must be a lot of clusters to randomise to avoid unequal distribution -need increased sample size of individuals -subjects within a cluster may be different to subjects in other clusters so ideal is lots of small clusters -analysis more complicated as need to take account of cluster design -allocation concealment more difficult
46
sampling frame | 6 mark short notes (only have 4 points rn)
-a sampling frame is a list of all the people forming a population from which a sample is taken -simple random sampling is when people in the group are allocated random numbers -the sampling frame comes from an initial group of interest from which individuals are selected -convenience samples are taken from a place that is convenient for that study
47
SMR | short notes
-standard mortality ratio -a measure, expressed as either a ratio or percentage to quantify an increase or decrease in mortality in a study cohort compared to the general population -calculated from expected deaths in a study population -compares observed deaths with expected deaths -needs number of persons in each age group in population being studied -age specific death rates of general population by same age groups -observed deaths in study population